Jens Schmidt

ORCID: 0000-0002-5589-2371
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About
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Research Areas
  • Inflammatory Myopathies and Dermatomyositis
  • Muscle Physiology and Disorders
  • Eosinophilic Disorders and Syndromes
  • Genetic Neurodegenerative Diseases
  • Skin Diseases and Diabetes
  • Neurogenetic and Muscular Disorders Research
  • Muscle and Compartmental Disorders
  • Peripheral Neuropathies and Disorders
  • Immunodeficiency and Autoimmune Disorders
  • Systemic Sclerosis and Related Diseases
  • Parkinson's Disease and Spinal Disorders
  • Autoimmune Neurological Disorders and Treatments
  • Immunotherapy and Immune Responses
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Dysphagia Assessment and Management
  • T-cell and B-cell Immunology
  • Amyotrophic Lateral Sclerosis Research
  • Multiple Sclerosis Research Studies
  • Exercise and Physiological Responses
  • Aldose Reductase and Taurine
  • Hereditary Neurological Disorders
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Heterotopic Ossification and Related Conditions
  • RNA regulation and disease
  • Viral Infections and Immunology Research

Universitätsmedizin Göttingen
2016-2025

Medizinische Hochschule Brandenburg Theodor Fontane
2021-2025

University of Göttingen
2015-2025

Immanuel Krankenhaus
2021-2025

Policlinico San Matteo Fondazione
2024

Klinikum Brandenburg
2023

RWTH Aachen University
2018-2022

University Hospital Schleswig-Holstein
2021

University of Lübeck
2021

Medizinische Hochschule Hannover
2021

Aims The EuroMyositis Registry facilitates collaboration across the idiopathic inflammatory myopathy (IIM) research community. This inaugural report examines pooled data. Methods Cross-sectional analysis of IIM cases from 11 countries was performed. Associations between clinical subtypes, extramuscular involvement, environmental exposures and medications were investigated. Results Of 3067 cases, 69% female. most common subtype dermatomyositis (DM) (31%). Smoking more frequent in connective...

10.1136/annrheumdis-2017-211868 article EN cc-by Annals of the Rheumatic Diseases 2017-08-30

CD4+CD25+ regulatory T cells (T reg cells) play a key role in controlling autoimmunity and inflammation. Therefore, therapeutic agents that are capable of elevating numbers or increasing effector functions this cell subset highly desirable. In previous report we showed superagonistic monoclonal antibody specific for rat CD28 (JJ316) expands activates vivo upon short-term vitro culture. Here demonstrate application very low dosages the superagonist into normal Lewis rats is sufficient to...

10.1084/jem.20051060 article EN The Journal of Experimental Medicine 2005-08-01

High-dose glucocorticosteroid hormones are a mainstay in the treatment of relapses multiple sclerosis. We searched for way to deliver ultra high doses glucocorticosteroids CNS rats with experimental autoimmune encephalomyelitis (EAE) using novel formulation polyethylene glycol (PEG)-coated long-circulating liposomes encapsulating prednisolone (predni solone liposomes, PL). 3H-labelled PL showed selective targeting inflamed CNS, where up 4.5-fold higher radioactivity was achieved than healthy...

10.1093/brain/awg176 article EN Brain 2003-07-14

Distinct interrelationships between inflammation and β-amyloid-associated degeneration, the two major hallmarks of skeletal muscle pathology in sporadic inclusion body myositis (sIBM), have remained elusive. Expression markers relevant for these pathomechanisms were analysed biopsies sIBM, polymyositis (PM), dermatomyositis (DM), dystrophic non-myopathic as controls, cultured human myotubes. By quantitative PCR, a higher upregulation was noted mRNA-expression CXCL-9, CCL-3, CCL-4, IFN-γ,...

10.1093/brain/awn053 article EN Brain 2008-04-17
Saskia von Stillfried Roman D. Bülow Rainer Röhrig Peter Boor Jana Böcker and 95 more Jens Schmidt Pauline Tholen Raphael W Majeed Jan Wienströer Joachim Weis Juliane Bremer Ruth Knüchel Anna Breitbach Claudio Cacchi Benita Freeborn Sophie Wucherpfennig Oliver Spring Georg Braun Christoph Römmele Bruno Märkl Rainer Claus Christine Dhillon Tina Schaller Éva Sipos Klaus Hirschbühl Michael Wittmann Elisabeth Kling Thomas Kröncke Frank L. Heppner Jenny Meinhardt Helena Radbruch Simon Streit David Horst Sefer Elezkurtaj Alexander Quaas Heike Göbel Torsten Hansen Ulf Titze Johann Lorenzen Thomas Reuter Jaroslaw Woloszyn Gustavo Baretton Julia Hilsenbeck Matthias Meinhardt Jessica Pablik Linna Sommer O. Holotiuk Meike Meinel Nina Sophia Mahlke Iréne Esposito Graziano Domenico Luigi Crudele Maximilian Seidl Kerstin Amann Roland Coras Arndt Hartmann Philip Eichhorn Florian Haller Fabienne Lange Kurt Werner Schmid Marc Ingenwerth Josefine Rawitzer Dirk Theegarten Christoph G. Birngruber Peter J. Wild Elise Gradhand Kevin Smith Martin Werner Oliver Schilling Till Acker Stefan Gattenlöhner Christine Stadelmann Imke Metz Jonas Franz Lidia Stork Carolina Thomas Sabrina Zechel Philipp Ströbel Claudia Wickenhauser Christine Fathke Anja Harder Benjamin Ondruschka Eric Dietz Carolin Edler Antonia Fitzek Daniela Fröb Axel Heinemann Fabian Heinrich Anke Klein Inga Kniep Larissa Lohner Dustin Möbius Klaus Püschel Julia Schädler Ann-Sophie Schröder Jan‐Peter Sperhake Martin Aepfelbacher Nicole Fischer Marc Lütgehetmann Susanne Pfefferle Markus Glatzel

Autopsies are an important tool in medicine, dissecting disease pathophysiology and causes of death. In COVID-19, autopsies revealed e.g., the effects on pulmonary (micro)vasculature or nervous system, systemic viral spread, interplay with immune system. To facilitate multicentre autopsy-based studies provide a central hub supporting autopsy centres, researchers, data analyses reporting, April 2020 German COVID-19 Autopsy Registry (DeRegCOVID) was launched. The electronic registry uses...

10.1016/j.lanepe.2022.100330 article DE cc-by-nc-nd The Lancet Regional Health - Europe 2022-02-18

Abstract Background Human pluripotent stem cell‐derived muscle models show great potential for translational research. Here, we describe developmentally inspired methods the derivation of skeletal cells and their utility in tissue engineering with aim to model regeneration dystrophy vitro. Methods Key steps include directed differentiation human embryonic progenitors followed by primary secondary foetal myogenesis into three‐dimensional muscle. To simulate Duchenne muscular (DMD), a...

10.1002/jcsm.13094 article EN cc-by Journal of Cachexia Sarcopenia and Muscle 2022-10-18

Sporadic Inclusion Body Myositis (sIBM) is the most common acquired muscle disease in patients above 50 years of age. Apart from inflammation skeletal muscle, overexpression amyloid precursor protein (APP) and intracellular accumulation its proteolytic fragment beta-amyloid play a central role pathogenesis sIBM. In neurodegenerative disorders, similar aggregations aberrant proteins have recently been shown to be susceptible autophagic degradation. Therefore, we analyzed macroautophagy APP...

10.1002/ana.21115 article EN Annals of Neurology 2007-04-27

Macroautophagy, a homeostatic process that shuttles cytoplasmic constituents into endosomal and lysosomal compartments, has recently been shown to deliver antigens for presentation on major histocompatibility complex (MHC) class II molecules. Skeletal muscle fibers show high level of constitutive macroautophagy express MHC molecules upon immune activation. We found tumor necrosis factor-α (TNF-α), monokine overexpressed in inflammatory myopathies, led marked up-regulation skeletal myocytes....

10.1074/jbc.m110.159392 article EN cc-by Journal of Biological Chemistry 2010-10-28

To assess safety and feasibility of real-time (RT) MRI for evaluation dysphagia to compare this technique standard assessment by flexible endoscopic swallowing (FEES) videofluoroscopy (VF) in a cohort patients with inclusion body myositis (IBM).Using RT-MRI, FEES, VF, an unselected 20 IBM was studied as index disease uniform dysphagia. Symptoms were explored standardized tools including Swallowing-Related Quality Life Questionnaire (SWAL-QoL), Functional Rating Scale, Patient-Reported...

10.1212/wnl.0000000000003337 article EN Neurology 2016-10-22
Marc Dürr Gunnar Nissen Kurt‐Wolfram Sühs Philipp Schwenkenbecher Christian Geis and 95 more Marius Ringelstein Hans‐Peter Hartung Manuel A. Friese Max Kaufmann Michael P. Malter Marie Madlener Franziska S. Thaler Tania Kümpfel Makbule Şenel Martin Häusler Hauke Schneider Florian Then Bergh Christoph Kellinghaus Uwe K. Zettl Klaus‐Peter Wandinger Nico Melzer Catharina C. Groß Peter Lange Jens Dreyhaupt Hayrettin Tumani Frank Leypoldt Jan Lewerenz Alexander Finke Alexandra Philipsen Andeas Linsa Andre Dik Andrea Kraft Andreas Binder Andreas van Baalen Anna Gorsler Anne‐Katrin Pröbstel Annette Baumgärtner Armin Grau Astrid Blaschek Benjamin Wunderlich Bettina Balint Brigitte Wildemann Carsten Finke Catharina C. Groß Christian G. Bien Christian Geis Christian Urbanek Christine Strippel Christoph Kellinghaus Christoph Lehrich Christos Krogias Chung Ha-Yeun Claudia Sommer Constanze Mönig Corinna I. Bien Corinna Trebst Daniel Bittner Dirk Fitzner Dominique Endres Fatme Seval Ismail Felix Rosenow Felix von Poderwils Florian Then Bergh Frank Hoffmann Frank Leypoldt Franz Blaes Franziska S. Thaler Friedrich Ebinger George Trendelenburg Gernot Reimann Gunnar Nissen G Seidel Hans‐Peter Hartung Harald Prüß Hauke Schneider Hayretti Tumani Heinz Wiendl Hendrik Rohner Henning Stolze Ilya Ayzenberg Ina Schröder Ina-Isabelle Schmütz Jan Lewerenz Jens Dreyhaupt Jens Schaumberg Jens Schmidt Joachim Havla Johanna Maria Helena Rau Johannes Piepgras Jonathan Wickel Josef Priller Jost Obrocki Judith Wagner Jürgen Faiss Justina Dargvainiene Kai Siebenbrodt Karsten Witt Katharina Eisenhut Kathrin Doppler Kerstin Hellwig

<h3>Background and Objectives</h3> CSF in antibody-defined autoimmune encephalitis (AE) subtypes shows subtype-dependent degrees of inflammation ranging from rare often mild to frequent robust. AEs with NMDA receptor antibodies (NMDAR-E) leucine-rich glioma-inactivated protein 1 (LGI1-E) represent opposite ends this spectrum: NMDAR-E typically frequent/robust LGI1-E rare/mild inflammation. For a more in-depth analysis, we characterized findings acute, therapy-naive multicentric,...

10.1212/nxi.0000000000001086 article EN cc-by-nc-nd Neurology Neuroimmunology & Neuroinflammation 2021-10-25

The apoptosis-inducing effects of i.v. methylprednisolone were investigated as a possible method controlling inflammation in the CNS adoptive transfer-experimental autoimmune encephalomyelitis (AT-EAE) Lewis rats. Two pulses given at peak mild and severe disease. T-cell apoptosis was assessed on spinal cord cross-sections by morphology TUNEL staining. Concentrations measured serum, CSF tissue high-pressure liquid chromatography (HPLC). In EAE, 10 mg/kg increased significantly infiltration...

10.1093/brain/123.7.1431 article EN Brain 2000-07-01

Interactions between inducible co‐stimulatory molecule (ICOS) and ICOS‐ligand (ICOS‐L) are crucial for T‐cell co‐stimulation, effector cell differentiation memory CD8+ activation. Because in the muscle of patients with sporadic inclusion body myositis (sIBM) clonally expanded T cells invade major histocompatibility complex (MHC) class I‐expressing fibres, we investigated ICOS·ICOS‐L interactions correlated their expression perforin, a marker cytotoxic function by autoinvasive cells. The mRNA...

10.1093/brain/awh148 article EN Brain 2004-02-26

The present guidelines on dermatomyositis (DM) represent an excerpt from the interdisciplinary S2k myositis syndromes of German Society Neurology (available at www.awmf.org). cardinal symptom in DM is symmetrical proximal muscle weakness. Elevated creatine kinase, CRP or ESR as well electromyography and biopsy also provide important diagnostic clues. Pharyngeal, respiratory, cardiac, neck muscles may be affected. Given that approximately 30% patients develop interstitial lung disease,...

10.1111/ddg.12909 article EN JDDG Journal der Deutschen Dermatologischen Gesellschaft 2016-03-01

Sporadic inclusion body myositis is a severely disabling myopathy. The design of effective treatment strategies hampered by insufficient understanding the complex disease pathology. Particularly, nature interrelationships between inflammatory and degenerative pathomechanisms in sporadic has remained elusive. In Alzheimer's dementia, accumulation β-amyloid been shown to be associated with upregulation nitric oxide. Using quantitative polymerase chain reaction, an overexpression inducible...

10.1093/brain/aws046 article EN Brain 2012-03-21
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